A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1055n100



Internal ID22787142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6733555..6788217hg38UCSC Ensembl
chr11:6754786..6809448hg19UCSC Ensembl
chr11:6711362..6766024hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3854663
hg1954663
hg1854663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041634, nsv1038427
Samples
Known GenesOR2AG1, OR2AG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1055n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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